Skip to main content
guest
Join
|
Help
|
Sign In
SPL-work-group
Home
guest
|
Join
|
Help
|
Sign In
SPL-work-group
Wiki Home
Recent Changes
Pages and Files
Members
Home
All pages of this SPL Wiki
- Documents and References
- Training and Seminars
- Industry Survey
All Groups/ Subteams
FAQs / Q and As
DUNS Number FAQ
FAQ
PLR FAQ
UNII Codes FAQ
VetMed FAQ
Biologics Q-and-A
Drug Element Q&A
Drug Listing Q&A
Image Issues
Ingredients
PLR
PLR Recent Major Changes
New Materials and Updates
Wikispaces : SPL-work-group - all changes
home:
May 22, 2018
will do.
home:
May 22, 2018
Great, same as what I ...
home:
May 22, 2018
I reported to spl@hhs....
home:
May 22, 2018
May I ask who you repo...
home:
May 22, 2018
I haven't tried submit...
home:
May 22, 2018
I am still getting sam...
home:
May 21, 2018
Sure will!
home:
May 21, 2018
So you were getting th...
home:
May 21, 2018
I had this issue Frida...
home: Error message help for SPF OTC submission
May 18, 2018
I am submitting a NDC ...
IDMP
Edit
0
3
…
2
Tags
iso
product identification
Notify
RSS
Backlinks
Source
Print
Export (PDF)
IDMP and EVMPD
Links to IDMP presentations:
Links to EMA Medicinal Products and EVMPD information:
July 1 Notice
Detailed guidance v2
The EMA webpage contains the plans
for the EU implementation of electronic submission of medicinal product information:
http://www.ema.europa.eu/ema/index.jsp?curl=pages/regulation/general/general_content_000496.jsp&mid=WC0b01ac05803bf141
The documents for technical implementation are available at:
http://www.ema.europa.eu/ema/index.jsp?curl=pages/regulation/document_listing/document_listing_000336.jsp&mid=WC0b01ac0580410138
EudraVigilance website
http://eudravigilance.ema.europa.eu/highres.htm
Javascript Required
You need to enable Javascript in your browser to edit pages.
help on how to format text
Turn off "Getting Started"
Home
...
Loading...
IDMP and EVMPD
Links to IDMP presentations:
Links to EMA Medicinal Products and EVMPD information:
July 1 Notice
Detailed guidance v2
The EMA webpage contains the plans for the EU implementation of electronic submission of medicinal product information:
http://www.ema.europa.eu/ema/index.jsp?curl=pages/regulation/general/general_content_000496.jsp&mid=WC0b01ac05803bf141
The documents for technical implementation are available at:
http://www.ema.europa.eu/ema/index.jsp?curl=pages/regulation/document_listing/document_listing_000336.jsp&mid=WC0b01ac0580410138
EudraVigilance website http://eudravigilance.ema.europa.eu/highres.htm